A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036539



Internal ID19125758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107460953..107476508hg38UCSC Ensembl
Innerchr11:107331679..107347234hg19UCSC Ensembl
Innerchr11:106836889..106852444hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3815556
hg1915556
hg1815556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1273n100
Supporting Variantsnssv3519946, nssv3710744, nssv3516919, nssv3518881, nssv3504474, nssv3520490
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036539
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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